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WormBase Tree Display for Gene: WBGene00001844

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Name Class

WBGene00001844SMapS_parentSequenceK02E10
IdentityVersion1
NameCGC_namehid-1Person_evidenceWBPerson655
Sequence_nameK02E10.2
Molecular_nameK02E10.2a
K02E10.2a.1
CE04694
K02E10.2b
CE34327
K02E10.2b.1
Other_nameCELE_K02E10.2Accession_evidenceNDBBX284606
Public_namehid-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:25WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classhid
Allele (89)
Legacy_information[M Ailion] Hid, Aex, Unc
StrainWBStrain00022812
WBStrain00022816
RNASeq_FPKM (74)
GO_annotation (16)
Ortholog (36)
Structured_descriptionConcise_descriptionhid-1 encodes a putative transmembrane protein, evolutionarily conservedamong eukaryotes but unfamiliar, that is required for negative regulationof dauer formation, along with normal locomotion and defecation; HID-1 isparalogous to C47D12.2 and dymeclin (OMIM:607461); hid-1 is expressed inneurons of the head, tail, and ventral nerve cord; hid-1 mutations aresuppressed by akt-1 and daf-16 mutations, suggesting that HID-1 acts inthe insulin-signalling branch of dauer regulation.Paper_evidenceWBPaper00006103
Curator_confirmedWBPerson567
Date_last_updated06 Sep 2006 00:00:00
Automated_descriptionInvolved in several processes, including cellular response to carbon dioxide; defecation; and negative regulation of pharyngeal pumping. Located in several cellular components, including Golgi cisterna; cytosol; and neuron projection. Expressed in intestine; nervous system; and uv1. Human ortholog(s) of this gene implicated in developmental and epileptic encephalopathy 105. Is an ortholog of human HID1 (HID1 domain containing).Paper_evidenceWBPaper00065943
Curator_confirmedWBPerson324
WBPerson37462
Inferred_automaticallyThis description was generated automatically by a script based on data from the WS291 version of WormBase
Date_last_updated29 Nov 2023 00:00:00
Disease_infoPotential_modelDOID:0070391Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:15736)
Molecular_infoCorresponding_CDSK02E10.2a
K02E10.2b
Corresponding_transcriptK02E10.2a.1
K02E10.2b.1
Other_sequence (92)
Associated_featureWBsf647861
WBsf647862
WBsf655167
WBsf662527
WBsf1004349
WBsf1022475
WBsf235392
WBsf235393
Experimental_infoRNAi_resultWBRNAi00033864Inferred_automaticallyRNAi_primary
WBRNAi00049703Inferred_automaticallyRNAi_primary
WBRNAi00016452Inferred_automaticallyRNAi_primary
Expr_patternExpr112
Expr2675
Expr9227
Expr9303
Expr12462
Expr1015861
Expr1031086
Expr1153423
Expr2012412
Expr2030648
Drives_constructWBCnstr00007716
WBCnstr00007719
WBCnstr00008655
WBCnstr00008656
WBCnstr00010897
WBCnstr00013836
WBCnstr00013886
WBCnstr00036651
Construct_product (11)
Microarray_results (25)
Expression_cluster (121)
SAGE_tag (14)
Interaction (29)
Anatomy_functionWBbtf0873
WBbtf0874
WBbtf0875
WBbtf0876
WBbtf0877
WBbtf0878
Map_infoMapXPosition-14.941Error0.129101
Well_ordered
PositivePositive_cloneK02E10Author_evidenceAilion EMM
Inferred_automaticallyFrom sequence, transcript, pseudogene data
NegativeNegative_cloneK08H6Author_evidenceAilion EMM
Mapping_data2_point7125
7126
7127
Multi_point3973
3974
3975
3976
3977
4716
Pos_neg_data10606
Reference (20)
MethodGene